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Berberine alleviates inflammation and suppresses PLA2-COX-2-PGE2-EP2 pathway through targeting gut microbiota in DSS-induced ulcerative colitis.

Authors :
Yu, Hansheng
Zhang, Shaobao
Li, Ruiming
Ma, Chong
Zhang, Qian
Xia, Fan
Zhou, Benjie
Xie, Zhiyong
Liao, Ziqiong
Source :
Biochemical & Biophysical Research Communications. Feb2024, Vol. 695, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Berberine, isolated from Coptis chinensis and Phellodendron amurense , can attenuate colonic injury and modulate gut microbiota disorders in ulcerative colitis (UC). However, the mechanism and causal relationship between gut microbiota and the efficacy of Berberine on UC are still unclear, which were investigated by pseudo-germ-free (PGF) mice, 16S rRNA gene analysis and transcriptome analysis in this study. The results demonstrated that Berberine improved gut microbiota disorders, colon damage, tight-junction proteins, inflammatory and anti-inflammatory cytokines in DSS-induced colitis mice with intact gut microbiota but not in PGF mice. Besides, immune-related and inflammation-related pathways were closely related to the efficacy that Berberine alleviated colitis by regulating gut microbiota. Furthermore, Berberine reduced PGE2, PLA2, COX-2, Ptges, EP2 and p-Stat3 only in colitis mice with intact gut microbiota. In summary, our study confirms that Berberine inhibits PLA2-COX-2-PGE2-EP2 pathway in UC through gut microbiota, leading to the alleviation of inflammation in colon, which further elucidates the underlying mechanism and promotes the application of Berberine in UC. [Display omitted] • The efficacy of Berberine on UC relies on gut microbiota. • Berberine reduces PGE2 and inflammation in UC through gut microbiota. • Berberine inhibits PLA2-COX-2-PGE2-EP2 pathway in UC via gut microbiota. • Apply 16S rRNA gene and transcriptome analysis and pseudo-germ-free mice. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0006291X
Volume :
695
Database :
Academic Search Index
Journal :
Biochemical & Biophysical Research Communications
Publication Type :
Academic Journal
Accession number :
174840779
Full Text :
https://doi.org/10.1016/j.bbrc.2023.149411